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ATP1A2 information


ATP1A2
Identifiers
AliasesATP1A2, FHM2, MHP2, ATPase Na+/K+ transporting subunit alpha 2, DEE98, FARIMPD
External IDsOMIM: 182340; MGI: 88106; HomoloGene: 47947; GeneCards: ATP1A2; OMA:ATP1A2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000702

NM_178405

RefSeq (protein)

NP_000693

NP_848492

Location (UCSC)Chr 1: 160.12 – 160.14 MbChr 1: 172.1 – 172.13 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Sodium/potassium-transporting ATPase subunit alpha-2 is a protein which in humans is encoded by the ATP1A2 gene.[5][6]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000018625 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000007097 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "ATP1A2 - Sodium/potassium-transporting ATPase subunit alpha-2 precursor - Homo sapiens (Human) - ATP1A2 gene & protein". www.uniprot.org. Retrieved 9 April 2022.
  6. ^ "Entrez Gene: ATP1A2 ATPase, Na+/K+ transporting, alpha 2 (+) polypeptide".

and 9 Related for: ATP1A2 information

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ATP1A2

Last Update:

ATPase subunit alpha-2 is a protein which in humans is encoded by the ATP1A2 gene. The protein encoded by this gene belongs to the family of P-type cation...

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Familial hemiplegic migraine

Last Update:

less than 25% of cases, is caused by mutations in the Na+ /K+ -ATPase gene ATP1A2. FHM3 is a rare subtype of FHM and is caused by mutations in a sodium channel...

Word Count : 4222

ATPase

Last Update:

usually take two main conformations, E1 and E2. Na+/K+ transporting: ATP1A1, ATP1A2, ATP1A3, ATP1A4, ATP1B1, ATP1B2, ATP1B3, ATP1B4 Ca++ transporting: ATP2A1...

Word Count : 2143

Hemiplegic migraine

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suffer from Hemiplegic migraines may have mutations of the CACNA1A and the ATP1A2 genes. The ICHD classification and diagnosis of migraine distinguish 6 subtypes...

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Alternating hemiplegia of childhood

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ATP1A3. A small number of cases seem to be caused by a mutation in the ATP1A2 gene. Where the mutation is inherited, it has the autosomal dominant pattern...

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Spinocerebellar ataxia type 6

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childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2". Neuropediatrics. 35 (5): 293–6. doi:10.1055/s-2004-821082. PMID 15534763...

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Sporadic hemiplegic migraine

Last Update:

cases with permanent neurological deficits have also been noted. CACNA1A, ATP1A2 and SCNA1 are genes associated with hemipeligic migraines, although many...

Word Count : 444

CACNB4

Last Update:

"Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4". Headache. 46 (7): 1136–41. doi:10.1111/j.1526-4610...

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List of OMIM disorder codes

Last Update:

Alström syndrome; 203800; ALMS1 Alternating hemiplegia of childhood; 104290; ATP1A2 Alveolar capillary dysplasia with misalignment of pulmonary veins; 265380;...

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